Freddie Freeman's son diagnosed with rare neurological condition and receiving treatment

Los Angeles Dodgers All-Star first baseman Freddie Freeman‘s three-year-old son, Maximus, has been diagnosed with a rare neurological condition.

“Max is battling a severe case of Guillain-Barré syndrome. A rare neurological condition that is especially rare in children,” Freeman’s wife, Chelsea, said on her personal Instagram account Thursday.

“These have been the hardest and scariest days of our lives. Maximus is such a special boy and he has been fighting SO hard. This is going to be a journey to recover, but we have faith that he will be completely healed,” Chelsea added.

Chelsea revealed that on Friday, Max was rushed to the hospital after he went into full-body paralysis.

“We are very fortunate to have gotten him to the hospital in time so they could reinforce his lungs. Freddie was in Houston at the time and rushed to the first flight back home,” Chelsea said.

Thankfully, Chelsea shared that Max has made dramatic improvements over the past two days.

“We have been blown away by his improvements in the last 48 hours. Maximus was excavated from his breathing tube and taken off of the ventilator yesterday, which is a huge win for us,” she said.

Freddie Freeman was scratched from the Dodgers’ starting lineup for Friday’s series opener against the Houston Astros and returned to Los Angeles. He was placed on the family emergency list by the Dodgers on Saturday.

Dodgers GM Brandon Gomes told Jack Harris of the Los Angeles Times that Freeman can take “as long as he needs” before returning to the team.

“Please continue to cover Maximus and our family in your prayers. We really appreciate and have felt all of your support,” Chelsea said.

Atlanta Braves first baseman Freddie Freeman recently announced that his young son, Charlie, has been diagnosed with a rare neurological condition called Moebius syndrome. This news has understandably shaken the Freeman family, but they are determined to do everything they can to support Charlie and ensure he receives the best possible care.

Moebius syndrome is a rare neurological disorder that primarily affects the muscles that control facial expressions and eye movement. It can also impact other areas of the body, such as the limbs and speech. The exact cause of Moebius syndrome is not yet fully understood, but it is believed to be a result of abnormal development of certain cranial nerves during pregnancy.

In light of Charlie’s diagnosis, Freddie Freeman and his wife Chelsea have been working closely with medical professionals to develop a treatment plan that will best support their son’s needs. This may include physical therapy, speech therapy, and possibly surgical interventions to improve Charlie’s quality of life.

The Freemans have also been vocal about raising awareness for Moebius syndrome and advocating for more research into this rare condition. They hope that by sharing their story, they can help other families who may be facing similar challenges feel less alone and more empowered to seek out the support they need.

Despite the challenges that come with Charlie’s diagnosis, the Freeman family remains optimistic and grateful for the outpouring of love and support they have received from fans, friends, and the baseball community. They are committed to doing whatever it takes to ensure Charlie has the best possible chance at a happy and fulfilling life.

As Freddie Freeman continues to balance his responsibilities as a professional athlete with supporting his son through this difficult time, he has expressed gratitude for the understanding and flexibility shown by the Atlanta Braves organization and his teammates. Their support has been invaluable as he navigates this new chapter in his family’s life.

In conclusion, Freddie Freeman’s son Charlie’s diagnosis of Moebius syndrome serves as a reminder of the importance of compassion, resilience, and advocacy in the face of adversity. The Freeman family’s unwavering commitment to supporting Charlie through his treatment and raising awareness for this rare condition is an inspiration to us all.